Allele Registry

Canonical Allele Identifier: PA2825891696

Gene: NFE2L2 HGNC NCBI

ClinVar RCV:

RCV000418369

RCV000419012

RCV000424664

RCV000425738

RCV000430352

RCV000434952

RCV000436001

ClinVar Variation:

376462

HGVS (amino-acid)	Matching Registered Transcripts
NP_001138885.1:p.Asp13Tyr	CA16602896 NM_001145413.3:c.37G>T